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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 589579생성일: 2026년 10월 25일

Boron tribromide → Anacetrapib metabolite M1

https://huagongshe.com/reaction/589579

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참여 물질

역할이름HCID투입량
반응물Boron tribromideHCID 25134—
반응물2-Oxazolidinone, 5-[3,5-bis(trifluoromethyl)phenyl]-3-[[4'-fluoro-2'-methoxy-5'-(1-methylethyl)-4-(trifluoromethyl)[1,1'-biphenyl]-2-yl]methyl]-4-methyl-, (4S,5R)-HCID 49849451—
용매DichloromethaneHCID 6344—
생성물Anacetrapib metabolite M1HCID 1152741173.8%

반응 단계

A solution of 4S,5R)-5-(3,5-bis(trifluoromethyl)phenyl)-3-((4′-fluoro-5′-isopropyl-2′-methoxy-4-(trifluoromethyl)biphenyl-2-yl)methyl)-4-methyl-1,3-oxazolidin-2-one (54) [prepared by methods described in WO2007/005572] (1.4 g) in DCM (5 mL) was treated with BBr3 (0.9 mL) at 15-16° C. and the reaction mixture stirred for 1 hr. The mixture was quenched with ice and diluted with EtOAc (150 mL) The mixture was washed with water, sat'd NaHCO3 solution, and brine, dried (Na2SO4), filtered and the solvent concentrated under reduced pressure. The crude product was purified by chromatography on silica gel to give 1.01 g (60%) of 55. 1H NMR (CDCl3) δ: 7.85 (s, 1H), 7.75-7.62 (m, 4H), 7.42 (m, 1H), 6.96 (dd, 1H), 7.69 (dd, 1H), 5.64 (d, 0.5H), 5.39 (d, 0.5H), 4.92-4.80 (m, 1H), 4.18 (d, 0.5H), 3.99 (d, 0.5H), 3.85 (m, 0.5H), 3.75 (m, 0.5H), 3.19 (m, 1H), 1.17-1.25 (m, 6H), 0.57 (d, 1.5H), 0.45 (d, 1.5H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09233938B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-ad08eb0743b144e1bcbf4d0f406eab88
출처 메모uspto-grants-2016_01